TWI379840B - Polymerizable composition and its uses - Google Patents
Polymerizable composition and its uses Download PDFInfo
- Publication number
- TWI379840B TWI379840B TW097129379A TW97129379A TWI379840B TW I379840 B TWI379840 B TW I379840B TW 097129379 A TW097129379 A TW 097129379A TW 97129379 A TW97129379 A TW 97129379A TW I379840 B TWI379840 B TW I379840B
- Authority
- TW
- Taiwan
- Prior art keywords
- weight
- composition
- monomer
- formula
- acrylate
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 89
- 239000000178 monomer Substances 0.000 claims description 54
- 238000000576 coating method Methods 0.000 claims description 46
- 239000011248 coating agent Substances 0.000 claims description 44
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 24
- 239000012788 optical film Substances 0.000 claims description 24
- -1 decyl propyl Chemical group 0.000 claims description 15
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 239000011256 inorganic filler Substances 0.000 claims description 7
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 4
- 239000012965 benzophenone Substances 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 4
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 150000002430 hydrocarbons Chemical group 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 239000012748 slip agent Substances 0.000 claims description 2
- 229910052717 sulfur Chemical group 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 claims 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims 2
- YGVZXFKGXQBWPC-UHFFFAOYSA-N (1,2-dihydroxycyclohexyl)-phenylmethanone Chemical compound OC1CCCCC1(O)C(=O)C1=CC=CC=C1 YGVZXFKGXQBWPC-UHFFFAOYSA-N 0.000 claims 1
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 claims 1
- HLCKAPCJELMQHY-UHFFFAOYSA-N 2-methylprop-2-enoic acid prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CC(=C)C(O)=O HLCKAPCJELMQHY-UHFFFAOYSA-N 0.000 claims 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 claims 1
- SENCTEJGLSLEDY-UHFFFAOYSA-N C1C(C)O1.C(C=C)(=O)OCC(C)(COC(C=C)=O)C Chemical compound C1C(C)O1.C(C=C)(=O)OCC(C)(COC(C=C)=O)C SENCTEJGLSLEDY-UHFFFAOYSA-N 0.000 claims 1
- LONXMOFSHXADLT-UHFFFAOYSA-N COC1(CC2=CC3=CC=CC=C3C=C2C=C1)OC Chemical compound COC1(CC2=CC3=CC=CC=C3C=C2C=C1)OC LONXMOFSHXADLT-UHFFFAOYSA-N 0.000 claims 1
- XTSHFXZAYGLGEO-UHFFFAOYSA-N [decyl(phenyl)phosphoryl]benzene Chemical compound C=1C=CC=CC=1P(=O)(CCCCCCCCCC)C1=CC=CC=C1 XTSHFXZAYGLGEO-UHFFFAOYSA-N 0.000 claims 1
- YVKNYPWWGQMCBZ-UHFFFAOYSA-N [diphenylphosphoryl(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 YVKNYPWWGQMCBZ-UHFFFAOYSA-N 0.000 claims 1
- YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 claims 1
- 229960005164 acesulfame Drugs 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- JZMPIUODFXBXSC-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.CCOC(N)=O JZMPIUODFXBXSC-UHFFFAOYSA-N 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 239000010408 film Substances 0.000 description 19
- 230000000694 effects Effects 0.000 description 15
- 239000000758 substrate Substances 0.000 description 15
- 230000003287 optical effect Effects 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920005668 polycarbonate resin Polymers 0.000 description 3
- 239000004431 polycarbonate resin Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 239000000052 vinegar Substances 0.000 description 3
- 235000021419 vinegar Nutrition 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000004386 diacrylate group Chemical group 0.000 description 2
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000004626 polylactic acid Substances 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- NQXNYVAALXGLQT-UHFFFAOYSA-N 2-[4-[9-[4-(2-hydroxyethoxy)phenyl]fluoren-9-yl]phenoxy]ethanol Chemical compound C1=CC(OCCO)=CC=C1C1(C=2C=CC(OCCO)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 NQXNYVAALXGLQT-UHFFFAOYSA-N 0.000 description 1
- DBAMLKZZDQYENY-UHFFFAOYSA-N 2-[diphenylphosphoryl(phenyl)methyl]-1,3,5-trimethylbenzene Chemical compound CC1=C(C(C2=CC=CC=C2)P(C2=CC=CC=C2)(C2=CC=CC=C2)=O)C(=CC(=C1)C)C DBAMLKZZDQYENY-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 206010033557 Palpitations Diseases 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 229920000954 Polyglycolide Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- VZTQQYMRXDUHDO-UHFFFAOYSA-N [2-hydroxy-3-[4-[2-[4-(2-hydroxy-3-prop-2-enoyloxypropoxy)phenyl]propan-2-yl]phenoxy]propyl] prop-2-enoate Chemical compound C=1C=C(OCC(O)COC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OCC(O)COC(=O)C=C)C=C1 VZTQQYMRXDUHDO-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- CZRTVSQBVXBRHS-UHFFFAOYSA-N ethyl carbamate prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCOC(N)=O CZRTVSQBVXBRHS-UHFFFAOYSA-N 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 230000008832 photodamage Effects 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000004633 polyglycolic acid Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
Description
1379840 九、發明說明: 【發明所屬之技術領域】 本發明係關於一種可聚合組合物及一種包含由該可聚人 組合物所形成之塗層的光學膜,此光學膜可用於顯示器之 背光模組中作為増亮膜。 ° 【先刖技術】 液晶顯示器(Liquid Crystal Display,LCD),具有 _、 薄、短、小、低耗熱量、低耗電量、以及幾乎無輕射傷害 等優點,目前已逐步取代傳統陰極射線管…扣“曲汉叮 Tube ’ CRT)顯示器。 目前來說,在背光模組中利用各式各樣之光學膜來提高 面板輝度,已成為最經濟與簡便的產品開發方案,依此方 式不但不須更動任何元件設計,亦不須消耗額外能源且 可提高LCD面板亮度使光源做最有效率的發揮。 增党膜通常簡稱BEF(Brightness Enhancement Film)或稱 聚光膜,其可藉由在聚酯基材上,塗佈特殊壓克力樹脂塗 f ’利用高能量料線(UV)將其硬化成稜鏡微結構而製 得。增亮膜主要的功能在於藉由折射與内部全反射的作 用,將由導光板(Light Guide)發出至四面八方之散亂光線 收集並集中至約±35度的正視角(〇n_Axis)方向,以提高 LCD的輝度。 般㊉用之增冗膜係利用線性稜鏡柱狀結構來達到聚光 效果’然而,一般含線性棱鏡柱狀結構之增亮膜所產生的 折射光線,易與來自顯示器中其它臈片的反射或折射光 I32725.doc 1379840 線,或增亮膜本身的其它反射或折射光線,產生光學干涉 現象,導致在外觀上出現雲紋(moire)或者牛頓環 ^ 為此,美國專利第6,28M63號揭露_種具有圓弧形柱狀处 : 制增亮膜,其能進一步整合集光與擴散作用,達到集光 , 及勻光目的,且可避免光學干涉現象。此外’弧形柱狀結 構之增亮膜,同時也可減少棱鏡結構與其他膜片或面板: 間接觸所產生之到傷,增加耐磨性。但是弧形柱狀結構 • 肖亮膜會降低輝度,為彌補輝度之損失,-般改善: 選用較高制率之聚合物塗層。一般而言’聚合㈣層^ 膜之增亮效果越好,例…專利特開1379840 IX. Description of the Invention: [Technical Field] The present invention relates to a polymerizable composition and an optical film comprising a coating formed from the polymerizable composition, which can be used for a backlight module of a display As a bright film in the group. ° [First Technology] Liquid Crystal Display (LCD), which has the advantages of _, thin, short, small, low heat consumption, low power consumption, and almost no light damage, has gradually replaced traditional cathode ray. Tube...Bucks the "Quhan 'Tube ' CRT) display. At present, the use of a variety of optical films in the backlight module to improve the brightness of the panel has become the most economical and simple product development program, in this way not only No need to change any component design, no need to consume extra energy and increase the brightness of the LCD panel to make the light source work most efficiently. Zengfang film is often referred to as BEF (Brightness Enhancement Film) or concentrating film, which can be used in On the polyester substrate, a special acrylic resin coating is applied to harden it into a 稜鏡 microstructure using a high energy material line (UV). The main function of the brightness enhancement film is by refraction and internal total reflection. The effect is to collect the scattered light from all directions in the Light Guide and concentrate it in the direction of the positive viewing angle (〇n_Axis) of about ±35 degrees to improve the brightness of the LCD. The linear 稜鏡 columnar structure is used to achieve the concentrating effect. However, the refracted light generated by the brightness enhancing film of the linear prism columnar structure is generally easy to reflect or refract light with other cymbals from the display. I32725.doc 1379840 The line, or other reflected or refracted light of the brightness enhancing film itself, causes optical interference, resulting in the appearance of moire or Newtonian rings. For this reason, U.S. Patent No. 6,28M63 discloses a circular arc shape. Columnar: Brightening film, which can further integrate the light collecting and diffusing effects, achieve the purpose of collecting light and homogenizing, and avoid optical interference. In addition, the curved film structure can also be used as a brightness enhancement film. Reducing the prism structure and other diaphragms or panels: Injury caused by contact, increasing wear resistance. However, curved columnar structure • Xiaoliang film will reduce the brightness, to compensate for the loss of brightness, generally improve: Polymer coating of the rate. Generally speaking, the better the brightness enhancement effect of the polymer (four) layer ^ film, for example...
目前已知可藉由添加自素以獲得具有較高折射率 物塗層,然而’齒素之存在會造成環境污染。 ▲ D 美:專利第⑽591號揭示一種高折射率可聚合“ 物,利用添加4,4·-雙(甲基丙稀醯 。 ^ L n ) 一本硫醚(4 4, » b^ethacroyl thio)diphenyl sulfide)^ ^ 5 ; 但缺點為此種單體價格太過昂貴。 ’' 综上所述,提供-種無上述缺點且較為經濟之 聚合物塗層,以提供增亮膜 射率 者。 的效旱乃業界所殷切期盼 【發明内容】 赛此’本發明之主要目的為提供—種 合組合物。本發明之另一目的在於提供一種光學膜的:聚 含-基材及至少—層由此可聚合組合物所形成之塗層:? 132725.doc 1379840 光學膜其係用於顯示器之背光模組令作為增亮膜。 在參閱圖式及隨後描述之實施方式後,本發明所屬技術 領域中具有通常知識者當可輕易瞭解本發明之基本精神以 及本發明所採用之技術手段與較佳實施態樣。 【實施方式】 本文中所使用之用語僅為描述所述之實施態樣,並非用 以限制本發明保護範圍。舉例言之,說明書中所使用的用 語「一 j,除非文中另有明確之解釋,否則用語「一」係 涵蓋單數及多數形式。 具體而言’本發明提供一種可聚合組合物,其具有至少 1.53的高折射率,且包含: (a)至少一種具式⑴之單體:It is currently known to obtain a coating having a higher refractive index by adding a self-priming material, however, the presence of dentate causes environmental pollution. ▲ D US: Patent No. (10) 591 discloses a high refractive index polymerizable substance by adding 4,4·-bis(methyl propyl oxime. ^ L n ) a thioether (4 4, » b^ethacroyl thio ) diphenyl sulfide) ^ ^ 5 ; but the disadvantage is that the price of such a monomer is too expensive. '' In summary, provide a polymer coating that does not have the above disadvantages and is more economical to provide a brightness enhancement film rate. The effect of the drought is the industry's eagerly awaited [invention] The main purpose of the present invention is to provide a combination composition. Another object of the present invention is to provide an optical film: a poly-containing substrate and at least - a coating formed from the polymerizable composition: 132725.doc 1379840 An optical film for use as a brightness enhancement film for a backlight module of a display. The invention is described with reference to the drawings and the embodiments described hereinafter The basic spirit of the present invention and the technical means and preferred embodiments of the present invention can be easily understood by those skilled in the art. [Embodiment] The terminology used herein is merely describing the embodiment. Like, not to limit The scope of the invention is to be understood as being in the singular and "a" In particular, the present invention provides a polymerizable composition having a high refractive index of at least 1.53 and comprising: (a) at least one monomer of formula (1):
父1及又2係各自獨立為H4Cl-C4烷基,較佳係各自獨立 為為Η或甲基; γι、γ2、丫3及Υ4係各自獨立為η、C丨-C4烧基或ΟΗ, 較佳係各自獨立為Η或甲基;及 a及b係各自獨立為選自〇至$之整數,較佳係各自獨立 132725.doc 丄3/外41) 為選自1至3之整數;及 (b)—光起始劑。 上述式⑴單體為苟衍生物二丙_酸酿單體(fiu_e envatlve dl⑽ylate __〇’具有介於ΐ6ι〜w之高 折射率,因此可有效增加該可聚合組合物固化後所得塗: ,折射率4⑴單體之用量,以該可聚合組合物之總重量 计,為至W重量%,較佳重量%,更The parent 1 and the 2 series are each independently H4Cl-C4 alkyl, preferably each independently being a hydrazine or a methyl group; the γι, γ2, 丫3 and Υ4 systems are each independently η, C丨-C4 alkyl or hydrazine, Preferably, each of them is independently hydrazine or methyl; and a and b are each independently an integer selected from 〇 to $, preferably each independently 132725.doc 丄3/outer 41) is an integer selected from 1 to 3; And (b) - a photoinitiator. The monomer of the above formula (1) is an anthracene derivative dipropionic acid monomer (fiu_e envatlve dl(10)ylate__〇' has a high refractive index of ΐ6 to w, so that the coating obtained by curing the polymerizable composition can be effectively increased: The refractive index 4 (1) monomer is used in an amount of up to W% by weight, preferably % by weight, based on the total weight of the polymerizable composition.
重量。/。至25重量%’最佳為4重量。/〇至2〇重量%。一般而 言,當式⑴單體之用量小於,無法有效提升折 射率;當式(I)單體之用量大於5〇重量%時,所得之可聚合 組合物太過剛性(rigid),不易於塗佈。 較佳地,式⑴單體中,Xi、X2'Yi、Y2、Y3W“ 自獨立為Η或甲基,且a及b係各自獨立為選自丨至3之整 數。根據本發明之-具體實施例,該式⑴單體為具式⑹ 之單體:weight. /. Up to 25% by weight 'preferably 4% by weight. /〇 to 2〇% by weight. In general, when the amount of the monomer of the formula (1) is less than, the refractive index cannot be effectively increased; when the amount of the monomer of the formula (I) is more than 5% by weight, the resulting polymerizable composition is too rigid and is not easy to be used. Coating. Preferably, in the monomer of the formula (1), Xi, X2'Yi, Y2, Y3W "is independently from fluorene or methyl, and each of a and b is independently an integer selected from 丨 to 3. According to the invention - specific In an embodiment, the monomer of the formula (1) is a monomer having the formula (6):
可用於本發明可聚合組合物中之光起始劑(組份,係 經光照射後會產生自由基並透過自由基之傳遞而5丨發聚合 反應之化合物’其例如可選自以下群組:二苯▼酮 132725.doc 1379840 (benzophenone)、二苯乙醇酮(benz〇in)、二苯乙二酮 (benzil)、2,2-二甲氧基-1,2_二苯基乙酮(2 2_dimeth〇xy_ l,2-diphenylethan-l-〇ne)、1-羥基環己基苯基酮(bhyhoxy cyclohexyl phenyl ketone)、2,4,6-三甲基苯甲醯基二苯基 膦氧化物(2,4,6-trimethylbenzoyl diphenyl phosphine oxide; TPO)及其組合,較佳係二苯甲酮。 本發明之光起始劑用量並無特殊限制,可視需要依該可 聚合組合物所包含之可聚合單體之種類及其用量進行調 整° 一般而言’以該可聚合組合物之總重量計,為〇丨重 ®%至10重量%’較佳為〇1重量%至5重量%。 一般可聚合組合物都會添加一些單體或寡聚體作為交聯 劑(Crosshnking agent),可使在聚合時增加分子與分子間 之交聯度’使組合物易於固化,並可提升固化後塗層之硬 度。本發明可聚合組合物可視需要添加交聯劑(組份(c))以 增進本發明可聚合組合物之成膜性。上述交聯劑之種類係 為本發明所屬技術領域中具有通常知識者所熟知者,例如 但不限於丙烯酸酯,可用於本發明中的丙烯酸酯例如但不 限於.(甲基)丙稀酸醋;胺基甲酸自旨丙稀酸自旨(urethane acrylate) ’如脂肪族胺基甲酸酯丙烯酸酯(aliphatic urethane acrylate)、脂肪族胺基甲酸酯六丙烯酸酯 (aliphatic urethane hexaacrylate)或芳香族胺基曱酸i旨六丙 烯酸酯(aromatic urethane hexaacrylate);聚酯丙烯酸酯 (polyester acrylate) ’ 如.聚醋二丙烯酸醋(p〇iyester diacrylate),環氧丙烯酸ϊ旨(epoxy acrylate),如雙紛A環氧 132725.doc 1379840A photoinitiator (a component which is a compound which generates a radical after light irradiation and transmits a radical by a radical emission by light irradiation) which can be selected, for example, from the following group, can be used in the polymerizable composition of the present invention. : Diphenylheptone 132725.doc 1379840 (benzophenone), benzhydrin, benzil, 2,2-dimethoxy-1,2-diphenylethanone (2 2_dimeth〇xy_ l,2-diphenylethan-l-〇ne), 1-hydroxycyclohexyl phenyl ketone, 2,4,6-trimethylbenzhydryldiphenylphosphine oxide (2,4,6-trimethylbenzoyl diphenyl phosphine oxide; TPO) and combinations thereof, preferably benzophenone. The amount of the photoinitiator of the present invention is not particularly limited, and may be included in the polymerizable composition as needed. The type of the polymerizable monomer and the amount thereof are adjusted. Generally, it is preferably from 〇1% by weight to 5% by weight based on the total weight of the polymerizable composition. Generally, the polymerizable composition will add some monomers or oligomers as a cross-linking agent, which can be used in the polymerization. Increasing the degree of cross-linking between molecules and molecules at the same time makes the composition easy to cure and can increase the hardness of the cured coating. The polymerizable composition of the present invention may be added with a crosslinking agent (component (c)) as needed to enhance the present. The film-forming property of the inventive polymerizable composition. The type of the above-mentioned crosslinking agent is well known to those skilled in the art, such as, but not limited to, acrylate, and the acrylate which can be used in the present invention, for example, but not Limited to (meth)acrylic acid vinegar; urethane formic acid urethane acrylate - such as aliphatic urethane acrylate, aliphatic urethane hexamate Acryl urethane hexaacrylate or aromatic urethane hexaacrylate; polyester acrylate 'p. 〇 二 acrylate (p〇iyester diacrylate), epoxy Epoxy acrylate, such as double sided A epoxy 132725.doc 1379840
二丙烯酸酉旨(bisphenol-A epoxy diacrylate);紛酸環氧丙稀 酸酯(no volac epoxy acrylate);或其混合物。上述(甲基)丙 烯酸酯可具有二或多個官能基,較佳係為具多官能基者。 適用於本發明之(甲基)丙烯酸酯之實例,例如但不限於: 三丙二醇二(甲基)丙烯酸酯(tripropylene giyC〇i di(meth)acrylate)、1,4- 丁 二醇二(曱基)丙烯酸酯(14_ butanediol di(meth)acrylate)、1,6-己二醇二(甲基)丙稀酸 醋(1,6-hexanediol di(meth)acrylate)、聚乙二醇二(曱基)丙 烯酸酯(polyethyleneglycol di(meth)acrylate)、稀丙基化二 (甲基)丙烯酸環己酯(allylated cyclohexyl di(meth)acrylate)、二(甲基)丙烯酸異氰脲酸酯 (isocyanurate di(meth)acrylate) >乙氧基化三經甲基丙烧三 (甲基)丙稀酸酯(ethoxylated trimethylol propane tri(meth)acrylate)、丙氧基化甘油三(曱基)丙烯酸酯 (propoxylated glycerol tri(meth)acrylate) ' 三經曱基丙烧三 (甲基)丙烯酸西旨(trimethylol propane tri(meth)acrylate)、三 (丙稀氧乙基)異氰酸脱酯(tris(aeryloxyethyl) isocyanurate) 或彼等之混合物。 可用於本發明之組份(c)之市售丙烯酸酯包括:由 Sartomer公司生產,商品名為SR454®、SR494®、 SR9020®、SR9021® 或 SR9041®者;由 Eternal公司生產,商 品名為624-100®者;及由UCB公司生產,商品名為Ebecryl 600®、Ebecryl 830®、Ebecryl 3605® 或 Ebecryl 6700® 者 等。 -12- 132725.doc C.S3 重旦。^時对77 (c)之用量,以組合物總重量計,可為1 二至6〇重量%,較佳為1〇重量%至5〇重量%,更佳為” 重里/〇至40重量〇/〇。 旦-可聚合組合物之黏度係隨該組合物中所含組份、含 操作溫度等因+鐵叙 ^, A, ”文動。δ組合物黏度過高時,豆操作 =佳’不利於塗佈,且易發生流平性不良等缺點:根據 X明’可視需要於該可聚合組合物中添加一具式⑼之 :稀酸醋單體(組份⑷)產生稀釋作用,以調整可聚合組合 物之黏度。該式(II)單體結構如下: ch2 (II) 其中R3為具2至6個碳原子之鏈狀烴,其可視情況經一或 多個選自氧及硫之雜原子所間隔,及福⑴之整數。Bisphenol-A epoxy diacrylate; no volac epoxy acrylate; or a mixture thereof. The above (meth) acrylate may have two or more functional groups, preferably a polyfunctional group. Examples of (meth) acrylates suitable for use in the present invention, such as, but not limited to, tripropylene giyC〇i di(meth)acrylate, 1,4-butanediol di(meth)acrylate Acetylene (14_butanediol di(meth)acrylate), 1,6-hexanediol di(meth)acrylate, polyethylene glycol di(meth)acrylate Polyethyleneglycol di(meth)acrylate, allylated cyclohexyl di(meth)acrylate, isocyanurate di (meth)acrylate) >ethoxylated trimethylol propane tri(meth)acrylate, propoxylated glycerol tris(mercapto) acrylate ( Propoxylated glycerol tri(meth)acrylate) 'trimethylol propane tri(meth)acrylate, tris(propyleneoxyethyl)isocyanate (tris(aeryloxyethyl) ) isocyanurate) or a mixture of them. Commercially available acrylates useful in component (c) of the present invention include those manufactured by Sartomer under the trade designations SR454®, SR494®, SR9020®, SR9021® or SR9041®; manufactured by Eternal, under the trade name 624 -100®; and manufactured by UCB under the trade names Ebecryl 600®, Ebecryl 830®, Ebecryl 3605® or Ebecryl 6700®. -12- 132725.doc C.S3 Heavy Dan. The amount of 77 (c), based on the total weight of the composition, may be from 1 to 6% by weight, preferably from 1% to 5% by weight, more preferably from "weight/twist to 40 weight" 〇/〇. The viscosity of the denier-polymerizable composition is related to the components contained in the composition, the operating temperature, etc. + iron, A, "vintage". When the viscosity of the δ composition is too high, the bean operation=good is not conducive to coating, and the flatness is prone to be disadvantageous, etc.: according to X's need, a formula (9) can be added to the polymerizable composition: dilute acid The vinegar monomer (component (4)) produces a dilution to adjust the viscosity of the polymerizable composition. The monomer structure of the formula (II) is as follows: ch2 (II) wherein R3 is a chain hydrocarbon having 2 to 6 carbon atoms, which may optionally be separated by one or more heteroatoms selected from oxygen and sulfur, and (1) an integer.
r3—〇--〇 若添加時,±述組份⑷之用量,以該可聚合組合物之 %重里》1* ’為1重里%至8〇重量%,較佳8重量%至重量 % ’更佳12重量%至60重量%。 較佳地,該式(II)單體為具式(11〇之單體: 132725.docR3—〇—〇 When added, the amount of the component (4) is from 1% by weight to 1% by weight, preferably from 8% by weight to 8% by weight of the polymerizable composition. More preferably from 12% by weight to 60% by weight. Preferably, the monomer of formula (II) is a formula (11 〇 monomer: 132725.doc
(π,)。 -13- 1379840 本案發明人進一步發現添加式(ιι)之丙烯酸酯單體於本 發明可聚合組合物中,不但可調整組合物之黏度使其更利 於塗佈,同時所製得之組合物於固化後依然具有高折射率 之性質。(π,). -13- 1379840 The inventors have further discovered that the addition of an acrylate monomer of the formula (i) to the polymerizable composition of the present invention not only adjusts the viscosity of the composition to facilitate coating, but also produces a composition. It still has the property of high refractive index after curing.
本發明之可聚合組合物,也可視需要選擇其他適當之丙 烯酸酯類單體((組份(d-l))來產生稀釋作用。可用於本發明 中的組份(d-Ι)之丙烯酸酯類單體,例如但不限於:丙烯酸 酯、甲基丙烯酸酯、2-苯氧基乙基丙烯酸酯(2-phenoxyl ethyl acrylate)、 三經曱基丙烧三丙稀酸酉旨 (trimethylolpropane triacrylate)、2-(對-異丙苯基-苯氧基)-乙基丙浠酸酯(cumyl phenoxyl ethyl acrylate)、丙氧化新 戊二醇二丙烯酸 g旨(propoxylated neopentyl glycol diacrylate)、乙氧化三經曱基丙烧三丙烯酸酷(ethoxylated trimethylolpropane triacrylate)、丙氧化三經甲基丙烧三丙 埽酸酉旨(propoxylated trimethyloipropane triacrylate)、二季 戊四醇六丙烯酸 S旨(dipentaerythritol hexaacrylate; DPHA),及彼等之混合物所組成之群組。市售此類單體例 子包含:由Eternal公司生產、商品名為EM2108®、 EM210®、EM231®者。 若添加時,上述組份(d-1 ),以該可聚合組合物之總重量 計,為1重量°/〇至80重量%,較佳8重量%至70重量%,更佳 12重量%至60重量%。 為避免本發明之可聚合組合物的分子量過高,產生黏度 太大,亦可視需要同時選用組份(d)和組份(d-l)來達到稀 -14- 132725.doc i S] 1379840 釋效果。 為進一步提高折射率,以增加光學族之輝度’本發明組 合物可視需要添加具高折射率之式(in)之單體(組份(e)):In the polymerizable composition of the present invention, other suitable acrylate monomers ((component (dl)) may be selected as needed to produce a dilution effect. The acrylates of the component (d-Ι) which can be used in the present invention. Monomers such as, but not limited to, acrylate, methacrylate, 2-phenoxyl ethyl acrylate, trimethylolpropane triacrylate, 2-(p-Phenylphenyl-phenoxy) ethyl acrylate, propoxylated neopentyl glycol diacrylate, ethoxylated triacetate Ethoxylated trimethylolpropane triacrylate, propoxylated trimethyloipropane triacrylate, dipentaerythritol hexaacrylate (DPHA), and mixtures thereof Groups of such commercially available examples include those produced by Eternal, Inc. under the trade names EM2108®, EM210®, EM231®. Part (d-1), based on the total weight of the polymerizable composition, is from 1% by weight to 80% by weight, preferably from 8% by weight to 70% by weight, more preferably from 12% by weight to 60% by weight. It is avoided that the molecular weight of the polymerizable composition of the present invention is too high, and the viscosity is too large, and component (d) and component (dl) may be simultaneously selected as needed to achieve the effect of dilute-14-132725.doc i S] 1379840. In order to further increase the refractive index to increase the brightness of the optical group, the composition of the invention may optionally add a monomer of the formula (in) having a high refractive index (component (e)):
G—SG-S
(III) 其中’ X3及X4各自獨立為H' C1-C4烧基或鹵素,較佳係 Η、甲基或鹵素;c及d各自獨立為1至4之整數;及G係選 自下列基團:(III) wherein 'X3 and X4 are each independently H'C1-C4 alkyl or halogen, preferably hydrazine, methyl or halogen; c and d are each independently an integer from 1 to 4; and G is selected from the group consisting of group:
H2C=C—C :=C—( R4 八 / \ 0¾ 及 其中R4為H4C]-C4烷基,較佳為!^或甲基;及爪為〇至6 之整數。 較佳地’式(III)單體為具式(ΙΠ!)之單體: ? _/=sH2C=C—C :=C—( R4 八 / \ 03⁄4 and wherein R 4 is H 4 C]-C 4 alkyl, preferably !^ or methyl; and the claw is an integer from 〇 to 6. Preferably, III) The monomer is a monomer of the formula (ΙΠ!): ? _/=s
ch2 Η2〇=(ρ—C_S—、 /)—S- R4 (III.) 其中R4如本文先前所定義。 更佳地’式(III)單體為具式(mo之單體:Ch2 Η 2 〇 = (ρ - C_S -, /) - S - R4 (III.) wherein R4 is as previously defined herein. More preferably, the monomer of formula (III) is a monomer of the formula (mo:
(ΙΠ2) 132725.doc •15- 1379840 :添加時,式_單體之用量,以該可聚合組合物之總 重置汁,為1重量%至60重量%,較佳為15重量。至 %。 里 此外,本發明組合物亦可視需要添加任何習知添加劑, 改變其物理或化學性能。可用於本發明中之添加劑一般 • 可選自以下群組:無機填料、抗靜電劑、滑劑⑽p agent)、流平劑、消泡劑及其組合。(ΙΠ2) 132725.doc • 15- 1379840: When added, the amount of the monomer is from 1% by weight to 60% by weight, preferably 15% by weight based on the total weight of the polymerizable composition. to %. Further, the composition of the present invention may be added with any conventional additives as needed to change its physical or chemical properties. Additives useful in the present invention are generally selected from the group consisting of inorganic fillers, antistatic agents, slip agents (10) p agents), leveling agents, antifoaming agents, and combinations thereof.
• 為增進組合物固化後所形成之塗層之硬度,可視需要於 組合物中添加無機填料,以避免因聚光結構塌陷現象影塑 光學性質。此外,無機填料亦具有提升液晶顯示器面板: 亮度之功效。可使用於本發明之無機填料係為本發明 技術領域中具有通常知識者所熟知者,其例如但不限於氧 化辞、二氧化矽、鈦酸鳃、氧化錯、氧化銘、碳酸鈣、二 乳化鈦、硫酸約、硫酸鎖或其混合物,較佳為二“I 錯太二氧切、氧化鋅或其混合物。上述無機填料具 ,有約10奈米至約350夺米之柄" 、 奈米。 不未之粒徑大小,較佳㈣奈米至150 靜=添:抗靜電劑於可聚合組合物中,使其具有抗 靜電之效果,進而提高作業良率。可使用於本發明之 電劑係為本發明所屬技 靜 本甘ν ^ 7頁域中具有通常知識者所孰知 =’:例但不限於乙氧基甘油脂肪酸醋類、四級錄化人 、曰肪=何生物、環氧樹腊(如聚環氧 Γ—或其它醇類街生物(如聚乙醇醋或聚乙二醇:) 132725.doc 1379840 根據本發明之一較佳實施態樣,本發明之可聚合組合物 中添加寡聚體作為交聯劑,以增加分子與分子間之交聯度 及增加該可聚合組合物固化後所形成之塗層硬度,使塗層 硬度達50或50以上之鍾擺硬度,較佳為5〇至7〇之鍾擺硬 度。一般而言,當鍾擺硬度小於50時,塗層之耐磨性不 佳;當鍾擺硬度大於70時,則容易脆化。上述交聯劑之種 類係如本文先前所述者。 本發明之可聚合組合物可塗覆於一基材或一光學薄片 (Optical thin sheet)(例如任何習知擴散膜或聚光膜)上形成 塗層’以增加表面耐磨性(wear resistance)並提供優越的光 滑度(smoothness);且因本發明之可聚合組合物包含具有 高折射率之式(I)單體,,故可使所形成之塗層具有高折射 率。本發明塗層之折射率為至少153,較佳為153至 1.62’可有效提升光學薄片之輝度。 上述基材之材料可為任何本發明所屬技術領域具有通常 知識者所熟知者,例如玻璃或塑膠。上述塑膠基材可由一 或多個高分子樹脂層所構成。用以構成上述高分子樹脂層 之樹脂之種類並無特殊限制’其例如選自以下群組:聚酯 樹脂(polyester resin),如聚對苯二甲酸乙二酯 (polyethylene terephthalate,PET)或聚萘二曱酸乙二酯 (polyethylene naphthalate, PEN)、聚丙烯酸酯樹脂 (polyacrylate resin),如聚甲基丙烯酸甲酯(p〇iymethyl methacrylate, PMMA)、聚烯烴樹脂(p〇iy〇iefin resin),如 聚乙烯(PE)或聚丙烯(PP)、聚環稀烴樹脂(p〇iyCyCi〇〇lefin 132725.doc 17 Ϊ379840 resin)、聚醯亞胺樹脂(polyimide resin)、聚碳酸酯樹脂 (polycarbonate resin)、聚胺基甲酸 S旨樹脂(polyurethane resin)、三醋酸纖維素(triacetyl cellulose,TAC)、聚乳酸 (Polylactic acid)及其組合,但不以此為限。其中,較佳係 選自聚酯樹脂、聚碳酸酯樹脂及其組合;更佳係聚對苯二 甲酸乙二酯。基材之厚度通常取決於所欲製得之光學產品 的需求,一般為30微米至300微米。 • 根據本發明一較佳實施態樣,本發明所用之基材包含單 層或多層凹凸微結構層。上述之單層或多層凹凸微結構係 用以提供光學薄膜所欲之光學性質,其形式並無特殊限 制,可為任何本發明所屬技術領域中具有通常知識者所熟 知者,例如:具有擴散效果的擴散結構及/或具有聚光效 果之聚光層《上述單層或多層結構可與基材一起以一體成 开/方式製備,例如以壓印(emb〇ss)、射出(Injecti〇n)或雙軸 =等方法製得;或以任何習知方式於基材上進行加工後 製付,例如:將含微粒的膠液,以塗佈方式於基材上直接 形成-凹凸微結構層,或於基材上先塗佈一塗層再於节塗 層上雕刻所需之凹凸微結構。 L於此’本發明另提供—種光學膜,其包含由本發明之 可聚合組合物所形成之塗層,上述之塗層可以是—平面膜 或特疋微結構,例如擴散微結構或聚光微結構。 —圖1係本發明光學膜之一實施態樣之示意圖。如圖1所 丁本發明光學膜包含一基材1及-呈聚光結構之塗層2。 本發明光學臈之塗層厚度’ -般為1微米至100微米,較 132725.doc 1379840 佳為10微米至40微米。當塗層具有特定結構之形式時,塗 層厚度係以其結構的最高點計算。以圖1之光學膜為例, 塗層2之厚度如符號a所示。 根據本發明之一實施態樣,該塗層為聚光結構。本發明 φ • 光學臈之聚光結構為本發明所屬技術領域中具有通常知識 ”· 者所熟知者,其例如但不限於:規則或不規則的稜鏡柱狀 結構(即,三角柱狀)、弧形柱狀結構(即,柱狀結構之峰呈 φ 圓弧形式)、圓錐狀結構、立體角結構、橘瓣形塊.狀結 構、透鏡狀結構及膠囊狀結構、或其組合等,較佳為稜鏡 柱狀結構或弧形柱狀結構❶上述稜鏡柱狀結構及/或弧形 柱狀結構可為線性(丨inear)、折線型(zigzag)或曲線型 (serpentine),且相鄰之兩柱狀結構可平行或不平行。 本發明之光學膜可以任何本發明所屬技術領域中具有通 常知識者所習知之方式费4。礙仓_丨丄々 心乃式表以。舉例s之,可經由包含以下 步驟之方法製造: φ ⑴混°具式⑴之單體、光起始劑及視需要之具式(H)之 单體、交聯劑與其它添加劑,以形成一膠態可聚合組合 . 物; ⑺將步驟⑴所得之膠態可聚合組合物以適當之方式塗 佈於-基材_L ’形成―塗層’再制例如滚 上形成一稜鏡花紋;以及 昭 (3)固化上述塗層,此可例如於常溫或加熱下,對苴 射能量射線而達成。 〃 視需要,可重複進行上述各步驟,以獲得包含複數塗層 132725.doc •19· 之光學膜。 =免基材表面到傷而料膜片的光學性質可視需要 在基材相對於由本發明 , 5組合物所形成之塗層之另 狀 $成抗到層。上述抗刮層可為平滑狀或非平滑 mK7i^到層之厚度較佳係介於〇·5〜3〇微米之間,根據 標準方法測量,所得霧度為1%〜9〇% Γ40%。根據;ISK7136標準方法,测量本發明光學膜: 王先線透過率,本發明光學膜具有不低於60%之全光線透 過率,較佳為高於80%,更佳9〇%或9〇%以上。 2本發明之可聚合组合物所製得之光學膜具有至少M3 的间折射率’可提供良好之光學增益值;因塗層中不含 ,素’不會污染環境,故可有效解決先前技術所存在之問 題此外本發明之可聚合組合物流平性佳,且成本較低 具備經濟上之優勢。 以下實施例將針對本發明提供進一步之說明。 實施例1-11 根據以下描述之方式製備實施例1至11之光學膜,各實 施例配方之組成係如表1所列。 首先,將各組份以表1所列之重量比例混合,再於5〇〇c 之溫度下,以轉速1,〇〇〇 rpm攪拌,形成一膠態可聚合組合 物。 將此膠態可聚合組合物塗佈於一聚苯二甲酸乙二酯 (PET)基材上(型號U34®,T0RAY公司所生產),以形成塗 層,然後利用滾輪壓花方式於塗層上形成一稜鏡花紋。接 132725.doc -20. 1379840 著,於常溫下,以能量射線照射該塗層,使之固化。得到 具有厚度為25微米之塗層之光學膜。 表1 且份 ⑻ (b) (c) (d) (d-1) 實施例 (公克) (公克) (公克) (公克) (公克) 1 2.5 3 30 7.5 0 2 5.0 3 30 15.0 0 3 7.5 3 30 22.5 0 4 10.0 3 30 30.0 0 5 12.5 3 30 37.5 0 6 15.0 3 30 45.0 0 7 10.0 3 30 0 0 8 10.0 3 30 0 30 9(比較例) 0 3 30 0 0 1〇(比較例) 0 3 30 0 50 π(比較例) 0 3 30 30 0 (a) :式(I)單體(新中村公司所生產,a_BPEF)• To increase the hardness of the coating formed after curing of the composition, inorganic fillers may be added to the composition as needed to avoid optical properties due to collapse of the concentrating structure. In addition, the inorganic filler also has the effect of improving the brightness of the liquid crystal display panel: brightness. The inorganic fillers useful in the present invention are well known to those of ordinary skill in the art, such as, but not limited to, oxidative, cerium oxide, barium titanate, oxidized, oxidized, calcium carbonate, diemulsified. Titanium, sulfuric acid, sulfuric acid, or a mixture thereof, preferably two "I-too-tano-dioxide, zinc oxide or a mixture thereof. The above inorganic filler has a handle of about 10 nm to about 350 metre", Nai Not limited to the particle size, preferably (four) nanometer to 150 static = add: antistatic agent in the polymerizable composition, so that it has an antistatic effect, thereby improving the work yield. Can be used in the present invention The electric agent is the technical knowledge of the present invention. It is known to those who have the usual knowledge in the field of the page: ': but not limited to ethoxyglycerin fatty acid vinegar, four-level recorded person, fat = what creature Epoxy wax (e.g., polyepoxyhydrazine- or other alcoholic street organisms (e.g., polyglycolic acid or polyethylene glycol:) 132725.doc 1379840. According to a preferred embodiment of the present invention, the polymerizable of the present invention Adding oligomers as crosslinkers to the composition to increase molecules and molecules The degree of cross-linking and the hardness of the coating formed after curing of the polymerizable composition are such that the hardness of the coating reaches a pendulum hardness of 50 or more, preferably a pendulum hardness of 5 to 7 inches. In general, When the pendulum hardness is less than 50, the abrasion resistance of the coating is not good; when the pendulum hardness is greater than 70, it is easy to embrittle. The type of the above crosslinking agent is as described herein before. The polymerizable composition of the present invention can be Coating on a substrate or an optical thin sheet (such as any conventional diffusion film or concentrating film) to form a coating' to increase surface wear resistance and provide superior smoothness (smoothness) And because the polymerizable composition of the present invention comprises a monomer of the formula (I) having a high refractive index, the formed coating layer can have a high refractive index. The refractive index of the coating of the present invention is at least 153. Preferably, the 153 to 1.62' is effective for enhancing the brightness of the optical sheet. The material of the substrate may be any one of ordinary skill in the art to which the present invention pertains, such as glass or plastic. The plastic substrate may be one or more high. Molecular resin layer The type of the resin constituting the above polymer resin layer is not particularly limited. It is, for example, selected from the group consisting of polyester resins such as polyethylene terephthalate (PET). Or polyethylene naphthalate (PEN), polyacrylate resin, such as polymethyl methacrylate (PMMA), polyolefin resin (p〇iy〇iefin Resin, such as polyethylene (PE) or polypropylene (PP), polycyclic hydrocarbon resin (p〇iyCyCi〇〇lefin 132725.doc 17 Ϊ379840 resin), polyimide resin, polycarbonate resin (polycarbonate resin), polyurethane resin, triacetyl cellulose (TAC), polylactic acid (Polylactic acid) and combinations thereof, but not limited thereto. Among them, preferred are polyester resins, polycarbonate resins and combinations thereof; more preferably polyethylene terephthalate. The thickness of the substrate generally depends on the desired optical product to be produced, typically from 30 microns to 300 microns. • According to a preferred embodiment of the invention, the substrate used in the present invention comprises a single layer or a plurality of layers of textured microstructures. The above-mentioned single-layer or multi-layered textured microstructures are used to provide the desired optical properties of the optical film, and the form thereof is not particularly limited, and may be any one of ordinary skill in the art to which the present invention pertains, for example, having a diffusion effect. Diffusion structure and/or concentrating layer having a concentrating effect "The above single layer or multi-layer structure can be prepared together with the substrate in an integrated manner, for example, imprinting (emb〇ss), injection (Injecti〇n) Or a biaxial = method; or in any conventional manner, after processing on a substrate, for example, the microparticle-containing glue is directly formed on the substrate by a coating method - a concave-convex microstructure layer, Or coating a coating on the substrate and then engraving the desired concave and convex microstructure on the coating. Further, the present invention provides an optical film comprising a coating formed from the polymerizable composition of the present invention, which may be a planar film or a special microstructure, such as a diffusion microstructure or a concentrating light. microstructure. - Figure 1 is a schematic illustration of one embodiment of an optical film of the present invention. The optical film of the present invention comprises a substrate 1 and a coating 2 in a concentrating structure. The coating thickness of the optical crucible of the present invention is generally from 1 μm to 100 μm, preferably from 10 μm to 40 μm compared to 132,725.doc 1379840. When the coating has the form of a particular structure, the thickness of the coating is calculated as the highest point of its structure. Taking the optical film of Fig. 1 as an example, the thickness of the coating 2 is indicated by the symbol a. According to an embodiment of the invention, the coating is a concentrating structure. The φ • optical 聚 concentrating structure of the present invention is well known in the art to which the present invention pertains, such as, but not limited to, a regular or irregular columnar structure (i.e., triangular prism), Curved columnar structure (ie, the peak of the columnar structure is in the form of φ arc), conical structure, solid angle structure, orange-shaped block, lenticular structure, lenticular structure and capsule structure, or a combination thereof Preferably, the columnar structure or the curved columnar structure may be linear (丨inear), zigzag or serpentine, and the phase The adjacent two columnar structures may be parallel or non-parallel. The optical film of the present invention may be used in any manner known to those of ordinary skill in the art to which the present invention pertains. It can be produced by the method comprising the following steps: φ (1) mixing the monomer of the formula (1), the photoinitiator and, if necessary, the monomer of the formula (H), a crosslinking agent and other additives to form a gel. State polymerizable combination. (7) will step (1) The resulting colloidal polymerizable composition is applied in a suitable manner to the substrate_L' to form a "coating", for example, to form a pattern on the roll; and to cure the above coating, for example At normal temperature or under heating, the energy ray is achieved. 上述 If necessary, the above steps can be repeated to obtain an optical film containing a plurality of coatings 132725.doc •19· The optical properties of the film may be such that it is resistant to the substrate in relation to the coating formed by the composition of the present invention. The scratch-resistant layer may be smooth or non-smooth mK7i^ to the thickness of the layer. Preferably, the film is between 〇·5~3〇 microns, and the obtained haze is 1%~9〇% Γ40% according to the standard method. According to the standard method of ISK7136, the optical film of the invention is measured: Wang Xianxian transmittance, The optical film of the present invention has a total light transmittance of not less than 60%, preferably more than 80%, more preferably 9% by weight or more than 9% by weight. 2 The optical film obtained by the polymerizable composition of the present invention has At least M3's refractive index' provides good optical gain values; The present invention will provide further explanation for the present invention. The following embodiments will provide further explanation for the present invention. Examples 1-11 The optical films of Examples 1 to 11 were prepared in the manner described below, and the compositions of the respective examples were as listed in Table 1. First, the components were mixed in the weight ratios listed in Table 1, Further, at a temperature of 5 〇〇c, stirring at a rotation speed of 1, rpm to form a colloidal polymerizable composition. The colloidal polymerizable composition is coated on a polyethylene terephthalate (PET). The substrate (Model U34®, manufactured by T0RAY) was used to form a coating, which was then embossed by a roller to form a pattern on the coating. According to 132725.doc -20. 1379840, the coating is irradiated with energy rays at room temperature to cure it. An optical film having a coating having a thickness of 25 μm was obtained. Table 1 and parts (8) (b) (c) (d) (d-1) Examples (g) (g) (g) (g) (g) 1 2.5 3 30 7.5 0 2 5.0 3 30 15.0 0 3 7.5 3 30 22.5 0 4 10.0 3 30 30.0 0 5 12.5 3 30 37.5 0 6 15.0 3 30 45.0 0 7 10.0 3 30 0 0 8 10.0 3 30 0 30 9 (Comparative example) 0 3 30 0 0 1〇 (Comparative example) 0 3 30 0 50 π (Comparative example) 0 3 30 30 0 (a) : Formula (I) monomer (manufactured by Shin-Nakamura Co., a_BPEF)
(b) :光起始劑(汽巴公司所生產,1184®) (c) :父聯劑(長興公司所生產,624-1〇〇®) (d) .式(II)單體(新中村公司所生產,a_len1〇) (d-1):丙烯酸酯類單體(長興公司所生產,eM21〇⑧) 將上述各實施例之光學膜進行折射率試驗(使用Index InStrUmentS 公司提供之 AUTOMATIC REFRACTOMETER GPR11-3 7儀器),並將各該光學膜應用於司所提 供的22相邊式背光模組,進行輝度增益程度試驗(採用 132725.doc TOPCON公司提供之BMW儀器),所得結果如表2所 不(b): Photoinitiator (produced by Ciba, 1184®) (c): Parent agent (produced by Changxing Co., Ltd., 624-1〇〇®) (d). Formula (II) monomer (new Produced by Nakamura Co., Ltd., a_len1〇) (d-1): Acrylate monomer (produced by Changxing Co., Ltd., eM21〇8) The optical film of each of the above examples was subjected to a refractive index test (using AUTOMATIC REFRACTOMETER supplied by Index InStrUmentS) GPR11-3 7 instruments), and the optical film is applied to the 22-phase edge backlight module provided by the company for the luminance gain test (using the BMW instrument provided by 132725.doc TOPCON). The results are shown in Table 2. No
表2Table 2
匕由表2中實施例1至8之結果可知,本發明可聚合租人 物所形成之塗層之折射率均高於153,且塗層折射率愈 高’應用於背光模組時,其輝度增益程度愈高,可提供較 佳之聚光效果。 2. 由表1及2可知,比較例9至1〇之組合物因不含式⑴單 體,無法有效提升折射率。 3. 由表1可知,比較例11之組合物添加了具稀釋作用之 式(II)單體以改善其流平性;且根據表2之結果可知,相較 於比較例9及10之組合物,比較例丨1之組合物因加入式⑴) 單體,可略微提升折射率。然而,由表2所載比較例丨丨和 實施例4之結果可知,實施例4之組合物除添加式(π)單體 以改善其流平性之外尚含有式(I)單體’且相較於不含式⑴ 132725.doc -22- 1379840 單體比較例11之組合物,實施例4之組合物之折射率提升 效果更好。 4.由表1及表2所載實施例4、7及8之結果可知,添加式 ⑴單體之後’有無添加式(11)或組份(d_1}之單體,其折射 率提升效果相當。但是以黏度計測量實施例4、7及8之組 合物之黏度時,所得黏度分別為130cps、18〇cps及 lOOcps。可見,添加式(II)之單體及組份(心丨)之單體,可 進一步改善組合物之流平性,且不會影響式⑴單體提升塗 層折射率之功效。 上述實施例僅為例示性說明本發明之實施態樣,並闡述本發 明之技術特徵,而非用於限制本發明之保護範疇。任何熟悉本 技術者在不違背本發明之技術原理及精神下,可輕易完成之改 變或安排,均屬本發明所主張之範圍。因此,本發明之權利保 護範圍係如後附申請專利範圍所列。 【圖式簡單說明】 圖1為本發明光學膜之一實施態樣之示意圖。 【主要元件符號說明】 1 基材 2 塗層 a 厚度 132725.doc -23-From the results of Examples 1 to 8 in Table 2, it can be seen that the refractive index of the coating formed by the polymerizable renter of the present invention is higher than 153, and the higher the refractive index of the coating is, the brightness of the coating is applied to the backlight module. The higher the gain, the better the concentrating effect. 2. As is apparent from Tables 1 and 2, the compositions of Comparative Examples 9 to 1 did not effectively increase the refractive index because they did not contain the monomer of the formula (1). 3. As can be seen from Table 1, the composition of Comparative Example 11 was added with a monomer of formula (II) having a dilution effect to improve the leveling property thereof; and according to the results of Table 2, it was found that the combination was compared with Comparative Examples 9 and 10. The composition of Comparative Example 1 can slightly increase the refractive index by adding the monomer of the formula (1). However, from the results of Comparative Example 表 and Example 4 contained in Table 2, it is understood that the composition of Example 4 contains the monomer of the formula (I) in addition to the addition of the (π) monomer to improve the leveling property thereof. The composition of Example 4 has a better refractive index enhancement effect than the composition of Comparative Example 11 which does not contain the formula (1) 132725.doc -22-1379840. 4. From the results of Examples 4, 7 and 8 shown in Tables 1 and 2, it can be seen that the addition of the monomer of the formula (1) is accompanied by the presence or absence of the addition of the monomer of the formula (11) or the component (d_1). However, when the viscosity of the compositions of Examples 4, 7 and 8 was measured by a viscometer, the obtained viscosities were 130 cps, 18 〇 cps and 100 cps, respectively. It can be seen that the monomer and component (heart palpitations) of formula (II) are added. The monomer can further improve the leveling property of the composition without affecting the effect of the refractive index of the monomer of the formula (1). The above embodiments are merely illustrative of the embodiments of the present invention, and the technology of the present invention is illustrated. The features are not intended to limit the scope of the present invention. Any changes or arrangements that can be easily accomplished without departing from the technical spirit and spirit of the present invention are within the scope of the present invention. The scope of the invention is as set forth in the appended claims. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic view showing an embodiment of an optical film of the present invention. [Description of main components] 1 substrate 2 coating a thickness 132725.doc -23-
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TWI413832B (en) * | 2010-08-26 | 2013-11-01 | Daxin Materials Corp | Light guiding plate and light guiding material composition |
KR101639082B1 (en) * | 2010-10-20 | 2016-07-13 | 코오롱인더스트리 주식회사 | Photopolymerizable composition and optical sheet |
TWI495174B (en) * | 2010-12-30 | 2015-08-01 | Au Optronics Corp | Organic photovoltaic cell |
CN104144975B (en) * | 2012-02-25 | 2017-09-22 | 三菱化学株式会社 | Coated film |
CN103304416B (en) * | 2012-03-15 | 2015-03-04 | 比亚迪股份有限公司 | Ultraviolet light curing monomer and preparation method thereof, polymerizable composition, brightness enhancement film and backlight module |
KR102105717B1 (en) * | 2013-08-08 | 2020-04-28 | 주식회사 케이오씨솔루션 | Polymerizable composition for high refractive optical material and method of preparing the optical material |
JP6894662B2 (en) * | 2014-10-30 | 2021-06-30 | 大阪ガスケミカル株式会社 | Polarizing plate and manufacturing method of polarizing plate |
CN105093367B (en) * | 2015-08-11 | 2017-10-20 | 宁波长阳科技股份有限公司 | A kind of composite brightening film and preparation method thereof |
US11407196B2 (en) * | 2015-12-28 | 2022-08-09 | 3M Innovative Properties Company | Article with microstructured layer |
KR101955766B1 (en) * | 2016-09-28 | 2019-03-07 | 삼성에스디아이 주식회사 | Composition for antireflection film, antireflection film prepared from the same, polarizing plate comprising the same and optical display apparatus comprising the same |
CN109796563A (en) * | 2018-12-21 | 2019-05-24 | 宁波激智科技股份有限公司 | A kind of composition and a kind of brightness enhancement film and its application |
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CA2102378A1 (en) * | 1992-11-16 | 1994-05-17 | Huan K. Toh | Cross-linkable polymeric composition |
WO1997044372A1 (en) * | 1996-05-23 | 1997-11-27 | Sola International Holdings Ltd. | Uv curable high index vinyl esters |
US5932626A (en) * | 1997-05-09 | 1999-08-03 | Minnesota Mining And Manufacturing Company | Optical product prepared from high index of refraction brominated monomers |
US6777070B1 (en) * | 1998-10-14 | 2004-08-17 | Tomoegawa Paper Co., Ltd. | Antireflection material and polarizing film using the same |
JP3797223B2 (en) * | 1999-11-29 | 2006-07-12 | オムロン株式会社 | Light-resistant microlens array and resin composition used therefor |
TW200307733A (en) * | 2002-02-01 | 2003-12-16 | Natoco Co Ltd | Composition curable with actinic energy ray and use thereof |
KR100675412B1 (en) * | 2003-09-09 | 2007-01-29 | 다이니폰 인사츠 가부시키가이샤 | An optical sheet and a method for manufacturing the same |
EP2159262B1 (en) * | 2004-10-07 | 2013-04-03 | Hitachi Chemical Company, Ltd. | Optical waveguide comprising a resin film |
EP1830204B1 (en) * | 2004-12-20 | 2018-10-17 | Nikon Corporation | Close-bonded diffractive optical element, optical material used therefor |
KR100544824B1 (en) * | 2005-01-27 | 2006-01-24 | 주식회사 코오롱 | A composition for making of prism layer and prism film made by using the same |
CN101120269B (en) * | 2005-02-17 | 2010-06-16 | 3M创新有限公司 | Brightness enhancement film comprising polymerized organic phase having low glass transition temperature |
JP2007277467A (en) * | 2006-04-10 | 2007-10-25 | Sony Chemical & Information Device Corp | Curable resin composition |
JP4915523B2 (en) * | 2006-06-29 | 2012-04-11 | Jnc株式会社 | Polymerizable liquid crystal composition |
JP5206066B2 (en) * | 2007-03-28 | 2013-06-12 | Jnc株式会社 | Polymerizable liquid crystal composition |
US7446159B1 (en) * | 2007-09-20 | 2008-11-04 | Sony Corporation | Curable resin composition |
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